KR101759157B1 - Film-forming method for forming silicon oxide film - Google Patents
Film-forming method for forming silicon oxide film Download PDFInfo
- Publication number
- KR101759157B1 KR101759157B1 KR1020170061254A KR20170061254A KR101759157B1 KR 101759157 B1 KR101759157 B1 KR 101759157B1 KR 1020170061254 A KR1020170061254 A KR 1020170061254A KR 20170061254 A KR20170061254 A KR 20170061254A KR 101759157 B1 KR101759157 B1 KR 101759157B1
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- South Korea
- Prior art keywords
- oxide film
- film
- silicon
- tungsten
- seed layer
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 title claims abstract description 69
- 229910052814 silicon oxide Inorganic materials 0.000 title claims abstract description 63
- 238000000034 method Methods 0.000 title claims abstract description 48
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 claims abstract description 62
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 62
- 239000010937 tungsten Substances 0.000 claims abstract description 62
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims abstract description 46
- 229910001930 tungsten oxide Inorganic materials 0.000 claims abstract description 46
- FZHAPNGMFPVSLP-UHFFFAOYSA-N silanamine Chemical compound [SiH3]N FZHAPNGMFPVSLP-UHFFFAOYSA-N 0.000 claims abstract description 22
- 238000010438 heat treatment Methods 0.000 claims abstract description 8
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 59
- 229910052710 silicon Inorganic materials 0.000 claims description 59
- 239000010703 silicon Substances 0.000 claims description 59
- 239000007800 oxidant agent Substances 0.000 claims description 17
- 239000004065 semiconductor Substances 0.000 claims description 10
- BLRPTPMANUNPDV-UHFFFAOYSA-N Silane Chemical compound [SiH4] BLRPTPMANUNPDV-UHFFFAOYSA-N 0.000 claims description 7
- WZUCGJVWOLJJAN-UHFFFAOYSA-N diethylaminosilicon Chemical compound CCN([Si])CC WZUCGJVWOLJJAN-UHFFFAOYSA-N 0.000 claims description 6
- AWFPGKLDLMAPMK-UHFFFAOYSA-N dimethylaminosilicon Chemical compound CN(C)[Si] AWFPGKLDLMAPMK-UHFFFAOYSA-N 0.000 claims description 6
- BIVNKSDKIFWKFA-UHFFFAOYSA-N N-propan-2-yl-N-silylpropan-2-amine Chemical compound CC(C)N([SiH3])C(C)C BIVNKSDKIFWKFA-UHFFFAOYSA-N 0.000 claims description 5
- 239000002994 raw material Substances 0.000 claims description 5
- 229910000077 silane Inorganic materials 0.000 claims description 5
- 125000003277 amino group Chemical group 0.000 claims description 4
- UOERHRIFSQUTET-UHFFFAOYSA-N N-propyl-N-silylpropan-1-amine Chemical compound CCCN([SiH3])CCC UOERHRIFSQUTET-UHFFFAOYSA-N 0.000 claims description 3
- CGRVKSPUKAFTBN-UHFFFAOYSA-N N-silylbutan-1-amine Chemical compound CCCCN[SiH3] CGRVKSPUKAFTBN-UHFFFAOYSA-N 0.000 claims description 3
- KTVCEVRNDLRINB-UHFFFAOYSA-N N-silyldocosan-1-amine Chemical compound C(CCCCCCCCCCCCCCCCC)CCCCN[SiH3] KTVCEVRNDLRINB-UHFFFAOYSA-N 0.000 claims description 3
- 150000004678 hydrides Chemical class 0.000 claims description 3
- LUXIMSHPDKSEDK-UHFFFAOYSA-N bis(disilanyl)silane Chemical compound [SiH3][SiH2][SiH2][SiH2][SiH3] LUXIMSHPDKSEDK-UHFFFAOYSA-N 0.000 claims description 2
- GADSHBHCKVKXLO-UHFFFAOYSA-N bis(disilanylsilyl)silane Chemical compound [SiH3][SiH2][SiH2][SiH2][SiH2][SiH2][SiH3] GADSHBHCKVKXLO-UHFFFAOYSA-N 0.000 claims description 2
- LICVGLCXGGVLPA-UHFFFAOYSA-N disilanyl(disilanylsilyl)silane Chemical compound [SiH3][SiH2][SiH2][SiH2][SiH2][SiH3] LICVGLCXGGVLPA-UHFFFAOYSA-N 0.000 claims description 2
- QOGHHHRYUUFDHI-UHFFFAOYSA-N heptasilepane Chemical compound [SiH2]1[SiH2][SiH2][SiH2][SiH2][SiH2][SiH2]1 QOGHHHRYUUFDHI-UHFFFAOYSA-N 0.000 claims description 2
- GCOJIFYUTTYXOF-UHFFFAOYSA-N hexasilinane Chemical compound [SiH2]1[SiH2][SiH2][SiH2][SiH2][SiH2]1 GCOJIFYUTTYXOF-UHFFFAOYSA-N 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- CVLHDNLPWKYNNR-UHFFFAOYSA-N pentasilolane Chemical compound [SiH2]1[SiH2][SiH2][SiH2][SiH2]1 CVLHDNLPWKYNNR-UHFFFAOYSA-N 0.000 claims description 2
- PLUQSKKKNPNZCQ-UHFFFAOYSA-N tetrasiletane Chemical compound [SiH2]1[SiH2][SiH2][SiH2]1 PLUQSKKKNPNZCQ-UHFFFAOYSA-N 0.000 claims description 2
- VEDJZFSRVVQBIL-UHFFFAOYSA-N trisilane Chemical compound [SiH3][SiH2][SiH3] VEDJZFSRVVQBIL-UHFFFAOYSA-N 0.000 claims description 2
- SZMYSIGYADXAEQ-UHFFFAOYSA-N trisilirane Chemical compound [SiH2]1[SiH2][SiH2]1 SZMYSIGYADXAEQ-UHFFFAOYSA-N 0.000 claims description 2
- 229910052990 silicon hydride Inorganic materials 0.000 claims 1
- 238000011534 incubation Methods 0.000 abstract description 9
- 238000004904 shortening Methods 0.000 abstract description 2
- 239000007789 gas Substances 0.000 description 67
- 230000008569 process Effects 0.000 description 17
- 235000012431 wafers Nutrition 0.000 description 17
- 238000000151 deposition Methods 0.000 description 13
- 230000008021 deposition Effects 0.000 description 11
- 239000011261 inert gas Substances 0.000 description 11
- 230000007246 mechanism Effects 0.000 description 11
- 239000000758 substrate Substances 0.000 description 10
- 230000015572 biosynthetic process Effects 0.000 description 9
- 239000006185 dispersion Substances 0.000 description 8
- 238000010926 purge Methods 0.000 description 6
- 239000010453 quartz Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- CBENFWSGALASAD-UHFFFAOYSA-N Ozone Chemical compound [O-][O+]=O CBENFWSGALASAD-UHFFFAOYSA-N 0.000 description 3
- 229910004298 SiO 2 Inorganic materials 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000001590 oxidative effect Effects 0.000 description 3
- 229910021420 polycrystalline silicon Inorganic materials 0.000 description 3
- 229920005591 polysilicon Polymers 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 2
- 238000000231 atomic layer deposition Methods 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- 238000005229 chemical vapour deposition Methods 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- ZNOKGRXACCSDPY-UHFFFAOYSA-N tungsten trioxide Chemical compound O=[W](=O)=O ZNOKGRXACCSDPY-UHFFFAOYSA-N 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 1
- 229910021529 ammonia Inorganic materials 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 229910001882 dioxygen Inorganic materials 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 210000003141 lower extremity Anatomy 0.000 description 1
- 239000011553 magnetic fluid Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000002052 molecular layer Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 238000000197 pyrolysis Methods 0.000 description 1
- 238000003466 welding Methods 0.000 description 1
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- H01L21/18—Manufacture or treatment of semiconductor devices or of parts thereof the devices having potential barriers, e.g. a PN junction, depletion layer or carrier concentration layer the devices having semiconductor bodies comprising elements of Group IV of the Periodic Table or AIIIBV compounds with or without impurities, e.g. doping materials
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- H01L21/28506—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers
- H01L21/28512—Deposition of conductive or insulating materials for electrodes conducting electric current from a gas or vapour, e.g. condensation of conductive layers on semiconductor bodies comprising elements of Group IV of the Periodic Table
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Abstract
(과제) 텅스텐막 또는 산화 텅스텐막 상에 산화 실리콘막을 형성해도, 산화 실리콘막의 인큐베이션 시간을 단축하는 것이 가능한 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법을 제공하는 것이다.
(해결 수단) 피처리체 상에 텅스텐막 또는 산화 텅스텐막을 형성하는 공정 (스텝 1)과, 텅스텐막 또는 산화 텅스텐막 상에 시드층을 형성하는 공정(스텝 2)과, 시드층 상에 산화 실리콘막을 형성하는 공정(스텝 3)을 구비하고, 상기 시드층을 텅스텐막 또는 산화 텅스텐막 상에, 피처리체를 가열하고, 텅스텐막 또는 산화 텅스텐막의 표면에 아미노실란계 가스를 공급하여 형성한다. [PROBLEMS] To provide a method for forming a silicon oxide film on a tungsten film or a tungsten oxide film capable of shortening the incubation time of the silicon oxide film even when the silicon oxide film is formed on the tungsten film or the tungsten oxide film.
(Step 1) of forming a tungsten film or a tungsten oxide film on an object to be processed, a step (step 2) of forming a seed layer on a tungsten film or a tungsten oxide film, and a step of forming a silicon oxide film (Step 3). The seed layer is formed on a tungsten film or a tungsten oxide film by heating the object to be processed and supplying an aminosilane-based gas to the surface of the tungsten film or tungsten oxide film.
Description
본 발명은, 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법 및 성막 장치에 관한 것이다. The present invention relates to a method for forming a silicon oxide film on a tungsten film or a tungsten oxide film and a film forming apparatus.
반도체 장치의 제조 프로세스에 있어서, 텅스텐막 상에 산화 실리콘(SiO2)막을 형성하는 경우가 있다. In a manufacturing process of a semiconductor device, a silicon oxide (SiO 2 ) film may be formed on a tungsten film.
예를 들면, 특허문헌 1에는 텅스텐 등의 금속 상에, 산화 실리콘막을 형성하는 기술이 기재되어 있다. For example,
그러나, 텅스텐(W)막, 또는 산화 텅스텐(WO3)막 상에 산화 실리콘막을 성막하는 경우, 성막 초기 단계에 있어서, 텅스텐 또는 산화 텅스텐 표면으로의 실리콘 흡착 레이트가 느리기 때문에, 산화 실리콘막이 성장을 시작하기까지의 인큐베이션 시간이 길어진다는 사정이 있다. 인큐베이션 시간이 길기 때문에, 텅스텐 이외의 하지(base) 상에 형성되는 산화 실리콘막에 비교하여 막두께가 얇아지거나, 또한 성막 초기 단계와 같이 실리콘의 흡착이 불충분한 상태일 때, 산화제가 텅스텐에 직접 접촉하기 때문에 텅스텐이 산화되어, 산화 텅스텐이 증막(增膜)되어 버린다는 사정이 있다. However, when a silicon oxide film is formed on a tungsten (W) film or a tungsten oxide (WO 3 ) film, the rate of silicon adsorption to the tungsten or tungsten oxide surface is slow at the initial stage of film formation. There is a problem that the incubation time until the start is long. Since the incubation time is long, when the film thickness is thinner than that of the silicon oxide film formed on a base other than tungsten, or when the adsorption of silicon is insufficient as in the initial stage of film formation, Tungsten is oxidized due to contact, and tungsten oxide is increased.
본 발명은, 텅스텐막 또는 산화 텅스텐막 상에 산화 실리콘막을 형성해도, 산화 실리콘막의 인큐베이션 시간을 단축할 수 있는 것이 가능한 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법 및, 그 성막 방법을 실시하는 것이 가능한 성막 장치를 제공한다. The present invention relates to a method for forming a silicon oxide film on a tungsten film or a tungsten oxide film capable of shortening the incubation time of a silicon oxide film even when a silicon oxide film is formed on a tungsten film or a tungsten oxide film, A film forming apparatus capable of carrying out the present invention is provided.
본 발명의 제1 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법은, (1) 피처리체 상에 텅스텐막 또는 산화 텅스텐막을 형성하고, (2) 상기 피처리체를 가열하고, 상기 가열된 상기 피처리체에, 아미노실란계 가스를 공급하고, (3) 상기 아미노실란계 가스가 공급된 상기 피처리체에, 실리콘을 포함하는 실리콘 원료 가스와, 산화제를 포함하는 가스를 교대로 공급하여, 상기 텅스텐막 또는 산화 텅스텐막이 형성된 상기 피처리체 상에, 산화 실리콘막을 형성한다.A method for forming a silicon oxide film on a tungsten film or a tungsten oxide film according to a first embodiment of the present invention includes the steps of (1) forming a tungsten film or a tungsten oxide film on the object to be processed, (2) (3) supplying a silicon raw material gas containing silicon and a gas containing an oxidizing agent to the object to which the aminosilane-based gas has been supplied, alternately And a silicon oxide film is formed on the object to be processed on which the tungsten film or tungsten oxide film is formed.
본 발명의 제2 실시 형태에 따른 성막 장치는, 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막을 성막하는 성막 장치로서, 상기 텅스텐막 또는 산화 텅스텐막이 형성된 피처리체를 수용하는 처리실과, 상기 처리실 내에, 아미노실란계 가스 및 실리콘 원료 가스 중 적어도 한쪽, 또한 산화제를 포함하는 가스를 공급하는 가스 공급 기구와, 상기 처리실 내를 가열하는 가열 장치와, 상기 처리실 내를 배기하는 배기 장치와, 상기 가스 공급 기구, 상기 가열 장치, 상기 배기 장치를 제어하는 컨트롤러를 구비하고, 상기 컨트롤러가, 상기 처리실 내에 있어서, 상기 제1 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법이, 상기 피처리체에 대하여 행해지도록, 상기 가스 공급 기구, 상기 가열 장치, 상기 배기 장치를 제어한다.A film forming apparatus according to a second embodiment of the present invention is a film forming apparatus for forming a silicon oxide film on a tungsten film or a tungsten oxide film and includes a processing chamber for accommodating a workpiece on which the tungsten film or tungsten oxide film is formed, , A gas supply mechanism for supplying a gas containing at least one of an aminosilane gas and a silicon source gas and an oxidizing agent, a heating device for heating the inside of the process chamber, an exhaust device for exhausting the inside of the process chamber, And a controller for controlling the apparatus, the heating device, and the exhaust device, wherein the controller is configured so that the method for forming the silicon oxide film on the tungsten film or the tungsten oxide film according to the first embodiment in the processing chamber includes: The gas supply mechanism, the heating device, and the exhaust device are arranged so that the gas supply mechanism, And control.
본 발명에 의하면, 텅스텐막 또는 산화 텅스텐막 상에 산화 실리콘막을 형성해도, 산화 실리콘막의 인큐베이션 시간을 단축하는 것이 가능한 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법 및, 그 성막 방법을 실시하는 것이 가능한 성막 장치를 제공할 수 있다. According to the present invention, there is provided a method for forming a silicon oxide film on a tungsten film or a tungsten oxide film, which can shorten the incubation time of a silicon oxide film even when a silicon oxide film is formed on a tungsten film or a tungsten oxide film, and a film forming method Can be provided.
도 1의 (A)는 본 발명의 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법의 일 예를 나타내는 흐름도이다.
도 1의 (B)는 도 1의 (A) 중의 스텝 3의 일 예를 나타내는 흐름도이다.
도 2의 (A)∼(C)는 도 1의 (A) 및 (B)에 나타내는 시퀀스 중의 피처리체의 상태를 개략적으로 나타내는 단면도이다.
도 3은 퇴적 시간과 실리콘층의 막두께와의 관계를 나타내는 도면이다.
도 4는 도 3 중의 파선 테두리 A 내를 확대한 확대도이다.
도 5의 (A)는 도면 대용 사진(SEM)이다.
도 5의 (B)는 막두께를 나타낸 도면이다.
도 6의 (A)는 도면 대용 사진(SEM)이다.
도 6의 (B)는 막두께를 나타낸 도면이다.
도 7의 (A)는 도면 대용 사진(SEM)이다.
도 7의 (B)는 막두께를 나타낸 도면이다.
도 8의 (A)∼(C)는 반도체 집적 회로 장치 내의 구조체(게이트 전극)를 나타내는 단면도이다.
도 9의 (A)∼(C)는 스텝 3의 다른 예를 나타내는 흐름도이다.
도 10은 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법을 실시하는 것이 가능한 성막 장치의 일 예를 개략적으로 나타내는 단면도이다. 1 (A) is a flowchart showing an example of a method of forming a silicon oxide film on a tungsten film or a tungsten oxide film according to an embodiment of the present invention.
1 (B) is a flowchart showing an example of
2 (A) to 2 (C) are cross-sectional views schematically showing the state of an object to be processed in the sequence shown in Figs. 1 (A) and 1 (B).
3 is a diagram showing the relationship between the deposition time and the film thickness of the silicon layer.
Fig. 4 is an enlarged view of the inside of a broken line A in Fig. 3.
5 (A) is a photograph (SEM) for drawing.
FIG. 5B is a view showing the film thickness.
6 (A) is a photograph (SEM) for drawing.
6 (B) is a view showing a film thickness.
7 (A) is a photograph (SEM) for drawing.
7 (B) is a view showing the film thickness.
8A to 8C are cross-sectional views showing a structure (gate electrode) in a semiconductor integrated circuit device.
9 (A) to 9 (C) are flowcharts showing another example of the
10 is a cross-sectional view schematically showing an example of a deposition apparatus capable of carrying out a deposition method of a silicon oxide film on a tungsten film or a tungsten oxide film according to an embodiment.
(발명을 실시하기 위한 형태)(Mode for carrying out the invention)
(성막 방법) (Film forming method)
도 1의 (A)는 본 발명의 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법의 일 예를 나타내는 흐름도이고, 도 1의 (B)는 도 1의 (A) 중의 스텝 3의 일 예를 나타내는 흐름도이고, 도 2의 (A)∼(C)는, 도 1의 (A) 및 (B)에 나타내는 시퀀스 중의 피처리체의 상태를 개략적으로 나타내는 단면도이다.1 (A) is a flow chart showing an example of a method of forming a silicon oxide film on a tungsten film or a tungsten oxide film according to an embodiment of the present invention. Fig. 1 (B) And FIGS. 2A to 2C are cross-sectional views schematically showing the state of the object in the sequence shown in FIGS. 1A and 1B. FIG.
우선, 도 1의 (A) 중의 스텝 1에 나타내는 바와 같이, 피처리체 상에 텅스텐막 또는 산화 텅스텐막을 형성한다. 산화 텅스텐막으로서는, 피처리체 상에 직접 산화 텅스텐막을 형성하도록 해도 좋고, 피처리체 상에 형성된 텅스텐막의 표면 상에 형성된 자연 산화막이어도 좋다. 또한, 본 예에서는, 피처리체로서 반도체 웨이퍼, 예를 들면, 실리콘 웨이퍼(W)를 이용했다. 이 실리콘 웨이퍼(W)의 실리콘 기판(1) 상에, 본 예에서는 텅스텐막(2)을 형성했다(도 2의 (A)).First, as shown in
다음으로, 도 1의 (A) 중의 스텝 2에 나타내는 바와 같이, 텅스텐막(2) 상에 시드층(3)을 형성한다(도 2의 (B)). 본 예에서는 시드층(3)을 다음과 같이 하여 형성했다. Next, as shown in
우선, 텅스텐막(2)이 형성된 실리콘 웨이퍼(W)를 성막 장치의 처리실 내에 반입한다. 이어서, 처리실 내의 온도를 올리고, 텅스텐막(2)이 형성된 실리콘 웨이퍼(W)를 가열하고, 가열된 텅스텐막(2)의 표면에 아미노실란계 가스를 공급한다. 이에 따라, 텅스텐막(2)의 표면 상에 시드층(3)를 형성한다. First, the silicon wafer W on which the
아미노실란계 가스의 예로서는, Examples of the aminosilane-
BAS(부틸아미노실란) BAS (butylaminosilane)
BTBAS(비스터셔리부틸아미노실란)BTBAS (non-stearylbutylaminosilane)
DMAS(디메틸아미노실란)DMAS (dimethylaminosilane)
BDMAS(비스디메틸아미노실란)BDMAS (bisdimethylaminosilane)
TDMAS(트리디메틸아미노실란)TDMAS (tridimethylaminosilane)
DEAS(디에틸아미노실란)DEAS (diethylaminosilane)
BDEAS(비스디에틸아미노실란)BDEAS (bisdiethylaminosilane)
DPAS(디프로필아미노실란)DPAS (dipropylaminosilane)
DIPAS(디이소프로필아미노실란)DIPAS (diisopropylaminosilane)
등을 들 수 있다. 본 예에서는, DIPAS를 이용했다. And the like. In this example, DIPAS was used.
스텝 2에 있어서의 처리 조건의 일 예는, One example of the processing conditions in
DIPAS 유량 : 500sccmDIPAS flow rate: 500 sccm
처리 시간 : 5분Processing time: 5 minutes
처리 온도 : 25℃Processing temperature: 25 ° C
처리 압력 : 532Pa(4Torr)Process pressure: 532 Pa (4 Torr)
이다. 스텝 2의 공정을, 본 명세서에서는 이하, 프리플로우(preflow)라고 부른다.to be. The
스텝 2는, 실리콘 원료를 텅스텐막(2)에 흡착시키기 쉽게 하는 공정이다. 또한, 본 명세서에서는, 스텝 2에 있어서 시드층(3)을 형성한다고 기재되어 있지만, 실제로는 거의 성막되는 일은 없다. 시드층(3)의 두께는, 바람직하게는 단(單)원자층 레벨의 두께 정도인 것이 좋다. 구체적인 시드층(3)의 두께를 언급하면, 0.1nm 이상 0.3nm 이하이다.
다음으로, 도 1의 (A) 중의 스텝 3에 나타내는 바와 같이, 시드층(3) 상에 산화물막, 본 예에서는, 산화 실리콘막(4)을 형성한다(도 2의 (C)). Next, as shown in
스텝 3의 일 예를 도 1의 (B)에 나타낸다. 본 예에서는, 산화 실리콘막(4)의 성막에, 실리콘을 포함하는 실리콘 원료 가스와, 실리콘을 산화시키는 산화제를 포함하는 가스를 교대로 공급하면서 성막하는, 소위 ALD(Atomic Layer Deposition)법, 또는 MLD(Molecular Layer Deposition)법을 채용했다. 산화제로서는, O2, O3, H2O, 또는 그들을 플라즈마에 의해 활성화시킨 활성종을 들 수 있다. 본 예에서는, O2 플라즈마로 생성한 O 라디칼을 이용했다. An example of
우선, 스텝 31에 나타내는 바와 같이, 처리실 내에 불활성 가스, 예를 들면, 질소(N2) 가스를 공급하여, 아미노실란계 가스를 퍼지한다. First, as shown in step 31, an inert gas, for example, nitrogen (N 2 ) gas is supplied into the process chamber to purge the aminosilane-based gas.
다음으로, 스텝 32에 나타내는 바와 같이, 실리콘 원료 가스를 처리실 내에 공급하고, 시드층(3)에 실리콘층을 형성한다. 실리콘 원료 가스의 예로서는, 스텝 2에서 이용한 아미노실란계 가스 외에, 아미노기를 포함하지 않는 실란계 가스를 들 수 있다. 아미노기를 포함하지 않는 실란계 가스로서는,Next, as shown in step 32, a silicon raw material gas is supplied into the processing chamber, and a silicon layer is formed on the
SiH2 SiH 2
SiH4 SiH 4
SiH6 SiH 6
Si2H4 Si 2 H 4
Si2H6 Si 2 H 6
SimH2m +2(단, m은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물 및, Si m H 2m +2 (where m is a natural number of 3 or more)
SinH2n(단, n은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물 중 적어도 하나를 포함하는 가스를 들 수 있다. Si n H 2n (where n is a natural number of 3 or more).
또한, 본 예에서는 아미노실란계 가스, 예를 들면, DIPAS를 이용했다. In this example, an aminosilane-based gas, for example, DIPAS was used.
스텝 32에 있어서의 처리 조건의 일 예는, One example of the processing conditions in step 32 is:
DIPAS 유량 : 500sccmDIPAS flow rate: 500 sccm
처리 시간 : 0.1분Processing time: 0.1 minute
처리 온도 : 25℃Processing temperature: 25 ° C
처리 압력 : 532Pa(4Torr)Process pressure: 532 Pa (4 Torr)
이다. to be.
다음으로, 스텝 33에 나타내는 바와 같이, 처리실 내에 불활성 가스, 예를 들면, 질소 가스를 공급하여, 실리콘 원료 가스를 퍼지한다. Next, as shown in step 33, an inert gas, for example, nitrogen gas is supplied into the process chamber to purge the silicon source gas.
다음으로, 스텝 34에 나타내는 바와 같이, 산화제를 포함하는 가스를 처리실 내에 공급하고, 스텝 32에서 형성된 실리콘층을 산화하여, 산화 실리콘막(4)을 형성한다. 스텝 34에 있어서도, 산화제로서는, O2, O3, H2O 또는 그들을 플라즈마에 의해 활성화시킨 활성종을 들 수 있다. 본 예에서는, O2 플라즈마로 생성한 O 라디칼을 이용했다. Next, as shown in step 34, a gas containing an oxidizing agent is supplied into the processing chamber, and the silicon layer formed in step 32 is oxidized to form a
다음으로, 스텝 35에 나타내는 바와 같이, 처리실 내에 불활성 가스, 예를 들면, 질소 가스를 공급하여, 산화제를 포함하는 가스를 퍼지한다. Next, as shown in
다음으로, 스텝 36에 나타내는 바와 같이, 반복 회수가 설정 회수인지 아닌지를 판단한다. Next, as shown in step 36, it is determined whether or not the number of repetitions is the set number of times.
설정 회수에 도달하지 않은 경우(NO), 스텝 32로 되돌아가, 스텝 32 부터 스텝 35를 반복한다. If the set number of times has not been reached (NO), the process returns to step 32, and steps 32 to 35 are repeated.
설정 회수에 도달한 경우(YES), 도 1의 (A)에 나타내는 바와 같이, 처리 종료가 된다. When the set number of times has been reached (YES), the processing is ended as shown in Fig. 1 (A).
(인큐베이션 시간)(Incubation time)
도 3에, 퇴적 시간과 실리콘층의 막두께와의 관계를 나타낸다. 도 3에 나타내는 결과는 하지를 산화 실리콘(SiO2)으로 한 경우이지만, 하지가 산화 실리콘이어도, 텅스텐이어도, 산화 텅스텐이어도, 동일한 경향을 나타낸다. 왜냐하면, 프리플로우, 즉, 아미노실란계 가스가 열분해됨으로써 얻어진 시드층(3)은 하지 상에 형성되기 때문이다. 실리콘층은, 어디까지나 시드층(3) 상에 흡착되어 성막된다.Fig. 3 shows the relationship between the deposition time and the film thickness of the silicon layer. The results shown in Fig. 3 are obtained when the substrate is made of silicon oxide (SiO 2 ), but the same tendency is exhibited even if the substrate is silicon oxide, tungsten or tungsten oxide. This is because the free layer, that is, the
본 예에서 이용한 프리플로우에 있어서의 처리 조건은, The processing conditions in the free flow used in this example are as follows:
DIPAS 유량 : 500sccmDIPAS flow rate: 500 sccm
처리 시간 : 5분Processing time: 5 minutes
처리 온도 : 400℃Treatment temperature: 400 ° C
처리 압력 : 53.2Pa(0.4Torr)Process pressure: 53.2 Pa (0.4 Torr)
이다. to be.
마찬가지로, 본 예에서 이용한 실리콘층을 성막하기 위한 처리 조건은, Similarly, the processing conditions for forming the silicon layer used in this example are as follows:
모노실란 유량 : 500sccmMonosilane flow rate: 500 sccm
퇴적 시간 : 30분/45분/60분Deposition time: 30 minutes / 45 minutes / 60 minutes
처리 온도 : 500℃Treatment temperature: 500 ° C
처리 압력 : 53.2Pa(0.4Torr)Process pressure: 53.2 Pa (0.4 Torr)
이다. to be.
실리콘층의 막두께는, 퇴적 시간을 30분으로 했을 때, 45분으로 했을 때 및, 60분으로 했을 때의 3점에서 측정했다. The film thickness of the silicon layer was measured at three points when the deposition time was 30 minutes, when the deposition time was 45 minutes, and when it was 60 minutes.
도 3 중의 선 Ⅰ은, 프리플로우가 있는 경우, 선 Ⅱ는 프리플로우가 없는 경우의 결과를 나타낸다. 선 Ⅰ, Ⅱ는, 측정된 3개의 막두께를 최소 이승법으로 직선에 근사한 직선이며, 식은 다음과 같다. Line I in FIG. 3 shows the result when there is free flow, and line II shows the result when there is no free flow. Lines I and II are straight lines approximating a straight line by the least squares method, and the equations are as follows.
선 Ⅰ : y=17.572x-20.855 … (1)Line I: y = 17.572x-20.855 ... (One)
선 Ⅱ : y=17.605x-34.929 … (2)Line II: y = 17.605x-34.929 ... (2)
도 3에 나타내는 바와 같이, 프리플로우가 있는 경우, 프리플로우가 없는 경우에 비교하여 실리콘층의 막두께가 증가하는 경향이 명백해졌다. As shown in Fig. 3, in the case of free flow, it became clear that the film thickness of the silicon layer increased as compared with the case where there was no free flow.
상기 (1), (2)식을 y=0, 즉 실리콘층의 막두께를 “0”으로 했을 때, 선 Ⅰ, Ⅱ와 퇴적 시간의 교점을 구한 것을 도 4에 나타낸다. 또한, 도 4는 도 3 중의 파선 테두리 A 내를 확대한 확대도이다. Fig. 4 shows the intersection of the line I and II and the deposition time when the above equations (1) and (2) are expressed by y = 0, that is, the film thickness of the silicon layer is " 0 ". Fig. 4 is an enlarged view of the inside of a broken line A in Fig. 3.
도 4에 나타내는 바와 같이, 프리플로우가 있을 때, 실리콘층의 퇴적이 처리 개시로부터 약 1.2분(x≒1.189)로부터 시작된다. 이에 대하여, 프리플로우가 없는 실리콘층일 때에는, 실리콘층의 퇴적이 처리 개시로부터 약 2.0분(x≒1.984)로부터 시작된다. As shown in Fig. 4, when there is free flow, deposition of the silicon layer starts from about 1.2 minutes (x? 1.189) from the start of the treatment. On the contrary, when the silicon layer has no free flow, deposition of the silicon layer starts from about 2.0 minutes (x? 1.984) from the start of the treatment.
이와 같이, 하지에 대하여 아미노실란계 가스의 프리플로우를 행함으로써, 인큐베이션 시간을, 약 2.0분으로부터 약 1.2분으로 단축할 수 있다.Thus, by performing the free flow of the aminosilane-based gas against the lower limb, the incubation time can be shortened from about 2.0 minutes to about 1.2 minutes.
(산화 실리콘막의 SEM 관찰) (SEM observation of silicon oxide film)
다음으로, 산화 실리콘막을 SEM 관찰한 결과를 나타낸다. Next, the results of SEM observation of the silicon oxide film are shown.
도 5의 (A) 및 (B)는 상기 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법을 이용하여 산화 실리콘막(4)을 형성한 경우이고, 도 5의 (A)는 SEM 사진, 도 5의 (B)는 막두께를 나타낸 도면이다. 도 6의 (A) 및 (B)는 비교예이고, 프리플로우가 없는 경우이다. 산화 실리콘막(4)은 성막할 때의 반복 회수를 모두 20사이클로 하여 성막했다. 또한, 텅스텐막(2)의 표면 상에는, 쌍방 모두 얇은 산화 텅스텐(WO3)막(5)이 형성되어 있다. 이 산화 텅스텐막(5)은 대기 중의 산소와 접촉함으로써 자연스럽게 형성된 자연 산화막이다. 물론, 산화 텅스텐막(5)은 없어도 좋다. 5A and 5B show the case where the
도 5의 (A) 및 (B)에 나타내는 바와 같이, 상기 일 실시 형태에 의하면, 텅스텐막(2) 상에, 막두께 1.3nm의 산화 텅스텐막(5)을 통하여 막두께 3.9nm(시드층(3)의 산화막두께 포함)의 산화 실리콘막(4)이 형성된다. 5A and 5B, according to the embodiment described above, a
이에 대하여, 도 6의 (A) 및 (B)에 나타내는 바와 같이, 프리플로우가 없는 비교예에 의하면, 텅스텐막(2) 상에, 막두께 1.5nm의 산화 텅스텐막(5)을 통하여 막두께 3.0nm의 산화 실리콘막(4)밖에 형성되어 있지 않다. 6 (A) and 6 (B), according to the comparative example in which there is no free flow, a
이와 같이, 상기 일 실시 형태에 의하면, 프리플로우를 하지 않는 경우에 비교하여, 인큐베이션 시간이 단축되고, 동일한 20사이클이라도, 약 30% 막두께가 두꺼운 산화 실리콘막(4)을 텅스텐막(2) 상에 형성할 수 있었다. As described above, according to the embodiment described above, the incubation time is shortened and the
또한, 상기 일 실시 형태에 의하면, 산화 텅스텐막(5)의 막두께가 1.3nm이지만, 비교예에서는, 산화 텅스텐막(5)의 막두께가 1.5nm으로 증막되어 있다. Further, according to the above embodiment, the film thickness of the
이 점에서, 상기 일 실시 형태에 의하면, 텅스텐막(2) 상으로의 산화 실리콘막(4)의 성막시에 있어서, 계면의 산화 텅스텐막(5)의 증막도 억제할 수 있다는 이점도 함께 얻을 수 있다. 이것은, 상기 일 실시 형태에서는, 시드층(3)이 텅스텐막(2)의 표면 상에 형성되기 때문에, 산화제가 직접적으로 텅스텐막(2)이나 산화 텅스텐막(5)에 접촉하는 것을 억제할 수 있기 때문이라고 생각된다. In this regard, according to the embodiment described above, it is also possible to obtain the advantage that the film thickness of the
도 7의 (A) 및 (B)는 실리콘 기판(1) 상에 산화 실리콘막(4)을 형성한 경우이고, 도 7의 (A)는 SEM 사진, 도 7의 (B)는 막두께를 나타낸 도면이다. 본 예에 있어서, 산화 실리콘막(4)은 처리 조건을 동일하게 하고, 반복 회수도 20사이클로 동일하게 하여 성막했다. 또한, 실리콘 기판(1)의 표면 상에는 두께 1nm의 자연 산화막(SiO2)(6)이 형성되어 있다. 7A and 7B show the case where the
도 7의 (A) 및 (B)에 나타내는 바와 같이, 이 경우, 실리콘 기판(1) 상에, 자연 산화막(6)을 통하여 막두께 4.1nm의 산화 실리콘막(4)이 형성된다. In this case, as shown in Figs. 7A and 7B, a
이 점에서, 상기 일 실시 형태에 의하면, 다음과 같은 이점도 얻을 수 있다.In this respect, according to the above embodiment, the following advantages can also be obtained.
도 8의 (A)∼(C)는, 반도체 집적 회로 장치 내의 구조체, 예를 들면, 게이트 전극을 나타내는 단면도이다. 8A to 8C are cross-sectional views showing a structure, for example, a gate electrode in a semiconductor integrated circuit device.
도 8의 (A)에 나타내는 바와 같이, 게이트 전극 중에는 폴리실리콘층(7) 상에 텅스텐막(2)을 적층한, 소위 폴리메탈 구조의 게이트 전극이 있다. 이 폴리메탈 구조의 게이트 전극의 측벽 상에, 산화 실리콘막(4)을 형성하는 경우, 프리플로우가 없는 경우에는, 산화 실리콘막(4)의, 폴리실리콘층(7) 상의 막두께와 텅스텐막(2) 상의 막두께와의 차이가 커진다(도 8의 (B)). 예를 들면, 도 6의 (B)에 나타낸 바와 같이, 프리플로우가 없는 비교예에서는, 산화 실리콘막(4)의 막두께는 텅스텐막(2) 상에서 3.0nm였다. 이 때문에, 산화 실리콘막(4)의 막두께의 불균일이 커진다. As shown in Fig. 8A, there is a so-called poly-metal gate electrode in which a
이에 대하여, 도 5의 (B)에 나타낸 바와 같이, 상기 일 실시 형태에 의하면, 산화 실리콘막(4)의 막두께는 텅스텐막(2) 상에서 3.9nm였다. 이 때문에, 산화 실리콘막(4)의, 폴리실리콘층(7) 상의 막두께와 텅스텐막(2) 상의 막두께의 차이를 비교예에 비교하여 작게 할 수 있다(도 8의 (C)). On the other hand, as shown in FIG. 5B, according to the above embodiment, the thickness of the
이와 같이, 상기 일 실시 형태에 의하면, 인큐베이션 시간을 짧게 할 수 있고, 단시간 혹은 반복 사이클수가 적은 경우라도, 보다 두꺼운 막두께의 산화 실리콘막(4)을, 텅스텐막(2) 상에 형성할 수 있다는 이점에 더하여, 실리콘과 텅스텐의 쌍방이 노출되어 있는 바와 같은 반도체 집적 회로 장치 내의 구조체 상에 산화 실리콘막(4)을 형성한 경우에, 산화 실리콘막의 막두께를, 불균일을 작게 하는 것도 가능해진다는 이점도 얻을 수있다. As described above, according to the embodiment described above, the incubation time can be shortened and the
또한, 산화 실리콘막(4)의 성막시에 있어서, 계면의 산화 텅스텐막(5)의 증막도 억제할 수 있다. 이것은, 상기 일 실시 형태에 의하면, 산화 텅스텐막(5) 또는 텅스텐막(2)의 표면에 시드층(3)이 형성된다. 이 시드층(3)은, 산화 실리콘막(4)의 성막 중, 특히, 산화 실리콘막(4)의 성막 초기 단계에 있어서 산화제의 확산을 막는 장벽이 된다. 이 때문에, 산화 텅스텐막(5) 또는 텅스텐막(2)이, 산화제에 직접적으로 접촉하기 어려워져, 산화 텅스텐막(5)의 증막이 억제된다. Further, at the time of forming the
(성막 방법의 다른 예)(Another example of the film forming method)
다음으로, 텅스텐막 상으로의 산화물막의 성막 방법의 다른 예를 설명한다. Next, another example of a method for forming an oxide film on a tungsten film will be described.
도 9의 (A)∼(C)는, 도 1의 (B) 중의 스텝 3의 다른 예를 나타내는 흐름도이다. 9 (A) to 9 (C) are flowcharts showing another example of
(제1 예)(First example)
도 9의 (A)에 나타내는 바와 같이, 제1 예는 도 1의 (B)에 나타낸 스텝 32, 33과, 스텝 34, 35를 교체한 예이다. 이와 같이, 아미노실란계 가스를 퍼지(스텝 31)한 후, 산화제를 공급(스텝 34)하도록 해도 좋다. As shown in Fig. 9 (A), the first example is an example in which steps 32 and 33 shown in Fig. 1 (B) and steps 34 and 35 are replaced. As described above, the aminosilane-based gas may be purged (step 31), and then the oxidant may be supplied (step 34).
(제2 예)(Example 2)
도 9의 (B)에 나타내는 바와 같이, 제2 예는 아미노실란계 가스를 퍼지하는 공정을 생략하고, 아미노실란계 가스를 공급한 후, 소정의 처리 시간 경과 후, 실리콘 원료 가스를 공급하도록 한 예이다. 이와 같이, 아미노실란계 가스를 퍼지하는 공정은 생략하는 것도 가능하다. As shown in Fig. 9 (B), the second example is a process in which the step of purging the aminosilane-based gas is omitted, the silicon source gas is supplied after the lapse of the predetermined treatment time after supplying the aminosilane- Yes. Thus, the step of purging the aminosilane-based gas can be omitted.
(제3 예)(Third example)
도 9의 (C)에 나타내는 바와 같이, 제3 예는 산화 실리콘막(4)을, 실리콘을 포함하는 실리콘 원료 가스와, 실리콘을 산화시키는 산화제를 포함하는 가스를 동시에 공급하면서 성막하는, 소위 CVD(Chemical Vapor Deposition)법을 이용하여 성막하도록 한 예이다. 이와 같이, 산화 실리콘막(4)의 성막에는, CVD법을 이용하는 것도 가능하다. As shown in Fig. 9C, the third example is a so-called " CVD " method in which a
(성막 장치)(Film forming apparatus)
다음으로, 상기 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법을 실시하는 것이 가능한 성막 장치의 일 예를 설명한다.Next, an example of a film forming apparatus capable of performing a film forming method of a silicon oxide film on a tungsten film or a tungsten oxide film according to the above embodiment will be described.
도 10은, 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법을 실시하는 것이 가능한 성막 장치의 일 예를 개략적으로 나타내는 단면도이다. 10 is a cross-sectional view schematically showing an example of a deposition apparatus capable of carrying out a deposition method of a silicon oxide film on a tungsten film or a tungsten oxide film according to an embodiment.
도 10에 나타내는 바와 같이, 성막 장치(100)는 하단이 개구된 천정이 있는 원통체 형상의 처리실(101)을 갖고 있다. 처리실(101)의 전체는, 예를 들면, 석영에 의해 형성되어 있다. 처리실(101) 내의 천정에는, 석영제의 천정판(102)이 설치되어 있다. 처리실(101)의 하단 개구부에는, 예를 들면, 스테인리스 스틸에 의해 원통체 형상으로 형성된 매니폴드(103)가 O링 등의 시일 부재(104)를 통하여 연결되어 있다. As shown in Fig. 10, the
매니폴드(103)는 처리실(101)의 하단을 지지하고 있다. 매니폴드(103)의 하방으로부터는, 피처리체로서 복수매, 예를 들면, 50∼100매의 반도체 웨이퍼, 본 예에서는, 실리콘 웨이퍼(W)를 다단으로 재치 가능한 석영제의 웨이퍼 보트(105)가 처리실(101) 내에 삽입 가능하도록 되어 있다. 웨이퍼 보트(105)는 복수개의 지주(支柱; 106)를 갖고, 지주(106)에 형성된 홈에 의해 복수매의 실리콘 웨이퍼(W)가 지지되도록 되어 있다. The manifold 103 supports the lower end of the
웨이퍼 보트(105)는 석영제의 보온통(107)을 통하여 테이블(108) 상에 올려 놓여져 있다. 테이블(108)은, 매니폴드(103)의 하단 개구부를 개폐하는, 예를 들면, 스테인리스 스틸제의 덮개부(109)를 관통하는 회전축(110) 상에 지지된다. 회전축(110)의 관통부에는, 예를 들면, 자성 유체 시일(magnetic fluid seal; 111)이 설치되고, 회전축(110)을 기밀하게 시일하면서 회전 가능하게 지지하고 있다. 덮개부(109)의 주변부와 매니폴드(103)의 하단부와의 사이에, 예를 들면, O링으로 이루어지는 시일 부재(112)가 개설(介設)되어 있다. 이에 따라 처리실(101) 내의 시일성이 유지되어 있다. 회전축(110)은, 예를 들면, 보트 엘리베이터 등의 승강 기구(도시하지 않음)에 지지된 아암(113)의 선단(先端)에 부착되어 있다. 이에 따라, 웨이퍼 보트(105) 및 덮개부(109) 등은, 일체적으로 승강되어 처리실(101) 내에 대하여 삽입 이탈된다. The
성막 장치(100)는 처리실(101) 내에, 처리에 사용하는 가스를 공급하는 처리 가스 공급 기구(114)와, 처리실(101) 내에 불활성 가스를 공급하는 불활성 가스 공급 기구(115)를 갖고 있다. The
처리 가스 공급 기구(114)는, 아미노실란계 가스 공급원(117), 실리콘 원료 가스 공급원(118), 산화제를 포함하는 가스 공급원(119)을 포함하고 있다. 아미노실란계 가스의 일 예는 디이소프로필아미노실란(DIPAS), 실리콘 원료 가스의 일 예는 디이소프로필아미노실란(DIPAS), 산화제를 포함하는 가스의 일 예는 산소(O2) 가스이다. 또한, 아미노실란계 가스와 실리콘 원료 가스가 동일한 경우에는, 아미노실란계 가스 공급원(117) 및 실리콘 원료 가스 공급원(118)을 공용하고, 어느 한쪽만을 형성하도록 해도 좋다. The processing
불활성 가스 공급 기구(115)는, 불활성 가스 공급원(120)을 포함하고 있다. 불활성 가스는, 퍼지 가스 등에 이용된다. 불활성 가스의 일 예는 질소(N2) 가스이다. The inert gas supply mechanism 115 includes an inert
아미노실란계 가스 공급원(117)은, 유량 제어기(121a) 및 개폐 밸브(122a)를 통하여 분산 노즐(123)에 접속되어 있다. 분산 노즐(123)은 석영관으로 이루어지고, 매니폴드(103)의 측벽을 내측으로 관통하여 상방향으로 굴곡되어 수직으로 연장된다. 분산 노즐(123)의 수직 부분에는, 복수의 가스 토출공(124)이 소정의 간격을 사이에 두고 형성되어 있다. 아미노실란계 가스는, 각 가스 토출 공(124)으로부터 수평 방향으로 처리실(101) 내를 향하여 대략 균일하게 토출된다. The aminosilane-based
또한, 실리콘 원료 가스 공급원(118)도, 유량 제어기(121b) 및 개폐 밸브(122b)를 통하여, 예를 들면, 분산 노즐(123)에 접속된다. The silicon raw material
산화제를 포함하는 가스 공급원(119)은, 유량 제어기(121c) 및 개폐 밸브(122c)를 통하여, 분산 노즐(125)에 접속되어 있다. 분산 노즐(125)은 석영관으로 이루어지고, 매니폴드(103)의 측벽을 내측으로 관통하여 상방향으로 굴곡되어 수직으로 연장된다. 분산 노즐(125)의 수직 부분에는, 복수의 가스 토출공(126)이 소정의 간격을 두고 형성되어 있다. 암모니아를 포함하는 가스는, 각 가스 토출공(126)으로부터 수평 방향으로 처리실(101) 내를 향하여 대략 균일하게 토출된다. The
불활성 가스 공급원(120)은, 유량 제어기(121d) 및 개폐 밸브(122d)를 통하여, 노즐(128)에 접속되어 있다. 노즐(128)은, 매니폴드(103)의 측벽을 관통하고, 그의 선단으로부터 불활성 가스를, 수평 방향으로 처리실(101) 내를 향하여 토출시킨다. The inert
처리실(101) 내의 분산 노즐(123 및 125)과 반대측의 부분에는, 처리실(101) 내를 배기하기 위한 배기구(129)가 형성되어 있다. 배기구(129)는 처리실(101)의 측벽을 상하 방향으로 깎아냄으로써 가늘고 길게 형성되어 있다. 처리실(101)의 배기구(129)에 대응하는 부분에는, 배기구(129)를 덮도록 단면이“ㄷ”자 형상으로 성형된 배기구 커버 부재(130)가 용접에 의해 부착되어 있다. 배기구 커버 부재(130)는 처리실(101)의 측벽을 따라 상방으로 연장되어 있고, 처리실(101)의 상방에 가스 출구(131)를 규정하고 있다. 가스 출구(131)에는, 진공 펌프 등을 포함하는 배기 기구(132)가 접속된다. 배기 기구(132)는 처리실(101) 내를 배기함으로써 처리에 사용한 처리 가스의 배기 및, 처리실(101) 내의 압력을 처리에 따른 처리 압력으로 한다. An
처리실(101)의 외주에는 통체 형상의 가열 장치(133)가 설치되어 있다. 가열 장치(133)는 처리실(101) 내에 공급된 가스를 활성화함과 함께, 처리실(101) 내에 수용된 피처리체, 본 예에서는 실리콘 웨이퍼(W)를 가열한다. A
성막 장치(100)의 각 부의 제어는, 예를 들면, 마이크로프로세서(컴퓨터)로 이루어지는 컨트롤러(150)에 의해 행해진다. 컨트롤러(150)는, 오퍼레이터가 성막 장치(100)를 관리하기 위해 커맨드의 입력 조작 등을 행하는 키보드나, 성막 장치(100)의 가동 상황을 가시화하여 표시하는 디스플레이 등으로 이루어지는 유저 인터페이스(151)가 접속되어 있다. The control of each section of the
컨트롤러(150)에는 기억부(152)가 접속되어 있다. 기억부(152)는, 성막 장치(100)에서 행해지는 각종 처리를 컨트롤러(150)의 제어로 실현하기 위한 제어 프로그램이나, 처리 조건에 따라서 성막 장치(100)의 각 구성부에 처리를 실행시키기 위한 프로그램, 즉 레시피가 격납된다. 레시피는, 예를 들면, 기억부(152) 중의 기억 매체에 기억된다. 기억 매체는 하드디스크나 반도체 메모리이어도 좋고, CD-ROM, DVD, 플래시메모리 등의 가반성(portable type)인 것이어도 좋다. 또한, 다른 장치로부터, 예를 들면 전용 회선을 통하여 레시피를 적절히 전송시키도록 해도 좋다. 레시피는 필요에 따라서, 유저 인터페이스(151)로부터의 지시 등으로 기억부(152)로부터 읽혀지고, 읽혀진 레시피에 따른 처리를 컨트롤러(150)가 행함으로써, 성막 장치(100)는 컨트롤러(150)의 제어하에서 원하는 처리가 실시된다. The
본 예에서는, 컨트롤러(150)의 제어하에서, 상기 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법, 예를 들면, 도 1의 (A), 도 1의 (B), 도 9의 (A)∼(C)에 나타낸 스텝에 따른 처리를 순차 행한다. In this example, under the control of the
상기 일 실시 형태에 따른 텅스텐막 또는 산화 텅스텐막 상으로의 산화 실리콘막의 성막 방법은, 도 10에 나타내는 바와 같은 성막 장치(100)에 의해 실시할 수 있다. A method of forming a silicon oxide film on a tungsten film or a tungsten oxide film according to the embodiment described above can be performed by the
이상, 본 발명을 일 실시예에 따라서 설명했지만, 본 발명은 상기 일 실시 형태에 한정되는 일은 없고, 여러 가지 변형이 가능하다. 또한, 본 발명의 실시 형태는 상기 일 실시 형태가 유일한 실시 형태도 아니다. Although the present invention has been described with reference to the embodiment, the present invention is not limited to the above embodiment, and various modifications are possible. Further, the embodiment of the present invention is not the only embodiment.
예를 들면, 산화제에 산소 가스를 대신하여, H2O 가스나 오존(O3) 가스를 이용할 수도 있고, 오존 가스의 경우에는 산화제를 포함하는 가스 공급원(119)에 오존 가스를 발생시키는 오조나이저를 구비하도록 해도 좋다. For example, H 2 O gas or ozone (O 3 ) gas may be used instead of oxygen gas as the oxidizing agent. In the case of ozone gas, an ozone gas generating source .
또한, O2, O3, H2O를 플라즈마에 의해 활성화시키고, 이들을 활성화시킨 활성 종을 실리콘 웨이퍼(W) 등의 피처리체 상에 토출해도 좋다. 이 경우, 처리실(101) 내부에 플라즈마를 발생시키는 플라즈마 발생 기구를, 예를 들면, 처리실(101) 내부에 설치하도록 해도 좋다. In addition, O 2 , O 3 , and H 2 O may be activated by plasma, and the activated species may be ejected onto a workpiece such as a silicon wafer W or the like. In this case, a plasma generating mechanism for generating plasma in the
또한, 상기 실시 형태에서는, 실리콘 원료 가스로서 아미노실란계 가스를 설명했지만, 시드층(3) 상으로의 실리콘층의 형성시에 있어서는, 실란계 가스를 이용할 수도 있다. 그 중에서도, SimH2m +2(단, m은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물 및, SinH2n(단, n은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물에 대해서는, In the above-described embodiment, the aminosilane-based gas is described as the silicon source gas. However, silane-based gas may be used for forming the silicon layer on the
SimH2m +2(단, m은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물이, Si m H 2m +2 (where m is a natural number of 3 or more)
트리실란(Si3H8)Trisilane (Si 3 H 8 )
테트라실란(Si4H10)Tetrasilane (Si 4 H 10 )
펜타실란(Si5H12)Pentasilane (Si 5 H 12 )
헥사실란(Si6H14)Hexasilane (Si 6 H 14 )
헵타실란(Si7H16)Heptasilane (Si 7 H 16 )
중 적어도 하나로부터 선택되고, ≪ / RTI >
SinH2n(단, n은 3 이상의 자연수)의 식으로 나타나는 실리콘 수소화물이, Si n H 2n (where n is a natural number of 3 or more)
사이클로트리실란(Si3H6)Cyclotrisilane (Si 3 H 6 )
사이클로테트라실란(Si4H8)Cyclotetrasilane (Si 4 H 8 )
사이클로펜타실란(Si5H10)Cyclopentasilane (Si 5 H 10 )
사이클로헥사실란(Si6H12)Cyclohexasilane (Si 6 H 12 )
사이클로헵타실란(Si7H14)Cycloheptasilane (Si 7 H 14 )
중 적어도 어느 하나로부터 선택할 수도 있다. May be selected from at least one of them.
또한, 상기 일 실시 형태에서는 본 발명을 복수의 실리콘 웨이퍼(W)를 탑재하여 일괄하여 성막을 행하는 배치식의 성막 장치에 적용한 예를 나타냈지만, 이것에 한정하지 않고, 1매의 웨이퍼마다 성막을 행하는 매엽식의 성막 장치에 적용할 수도 있다. In the above-described embodiment, the present invention is applied to a batch type film forming apparatus in which a plurality of silicon wafers W are mounted to perform film formation in a batch. However, the present invention is not limited to this, The present invention can be applied to a single-wafer type film forming apparatus.
또한, 피처리체로서는, 반도체 웨이퍼에 한정되지 않고, LCD 유리 기판 등의 다른 기판에도 본 발명을 적용할 수 있다. In addition, the object to be processed is not limited to a semiconductor wafer, but the present invention can be applied to other substrates such as an LCD glass substrate.
그 외에, 본 발명은 그의 요지를 일탈하지 않는 범위에서 여러 가지로 변형할 수 있다. In addition, the present invention can be modified in various ways without departing from the gist of the present invention.
1 : 실리콘 기판
2 : 텅스텐막
3 : 시드층
4 : 산화 실리콘막1: silicon substrate
2: tungsten film
3: Seed layer
4: silicon oxide film
Claims (7)
실리콘 웨이퍼의 표면 상에 텅스텐막 또는 산화 텅스텐막을 형성하는 단계로서, 상기 텅스텐막 또는 산화 텅스텐막이 형성된 후에, 상기 텅스텐막 또는 산화 텅스텐막은 제1 노출면을 갖고, 상기 실리콘 웨이퍼는 제2 노출면을 갖는, 단계;
상기 제1 노출면 및 제2 노출면을 가열하는 단계;
가열된 상기 제1 노출면 및 제2 노출면 상의 모두에 아미노실란계 가스를 동시에 공급함으로써, 상기 제1 노출면 상에 제1 시드층을 형성하고, 상기 제2 노출면 상에 제2 시드층을 형성하는 단계로서, 상기 제1 시드층 및 상기 제2 시드층은 제1 실리콘층인, 단계; 및
상기 제1 시드층 및 제2 시드층 상에 실리콘을 포함하는 실리콘 원료 가스를 공급함으로써, 상기 제1 시드층 및 제2 시드층 상의 모두에 제2 실리콘층을 형성하고, 그리고 상기 제2 실리콘층 상에 산화제를 포함하는 가스를 공급함으로써, 상기 제1 시드층 및 제2 시드층 상의 모두에 산화 실리콘막을 형성하는 단계
를 포함하는 산화 실리콘막의 성막 방법.As a film forming method for forming a silicon oxide film,
Forming a tungsten film or a tungsten oxide film on the surface of a silicon wafer, wherein after the tungsten film or tungsten oxide film is formed, the tungsten film or tungsten oxide film has a first exposed surface, and the silicon wafer has a second exposed surface ;
Heating the first exposed surface and the second exposed surface;
A first seed layer is formed on the first exposed surface by simultaneously supplying aminosilane-based gas to both the first exposed surface and the second exposed surface heated, and the second seed layer is formed on the second exposed surface, Wherein the first seed layer and the second seed layer are a first silicon layer; And
Forming a second silicon layer on both the first seed layer and the second seed layer by supplying a silicon source gas containing silicon on the first seed layer and the second seed layer, Forming a silicon oxide film on both the first seed layer and the second seed layer by supplying a gas containing an oxidizing agent onto the first seed layer and the second seed layer
And a silicon oxide film.
상기 아미노실란계 가스가,
BAS(부틸아미노실란)
BTBAS(비스터셔리부틸아미노실란)
DMAS(디메틸아미노실란)
BDMAS(비스디메틸아미노실란)
TDMAS(트리디메틸아미노실란)
DEAS(디에틸아미노실란)
BDEAS(비스디에틸아미노실란)
DPAS(디프로필아미노실란) 및,
DIPAS(디이소프로필아미노실란)
중 적어도 하나를 포함하는 가스로부터 선택되는 것을 특징으로 하는 산화 실리콘막의 성막 방법.The method according to claim 1,
Wherein the aminosilane-
BAS (butylaminosilane)
BTBAS (non-stearylbutylaminosilane)
DMAS (dimethylaminosilane)
BDMAS (bisdimethylaminosilane)
TDMAS (tridimethylaminosilane)
DEAS (diethylaminosilane)
BDEAS (bisdiethylaminosilane)
DPAS (dipropylaminosilane), and
DIPAS (diisopropylaminosilane)
≪ / RTI > and a gas comprising at least one of the following.
상기 실리콘 원료 가스가, 아미노실란계 가스, 또는 아미노기를 포함하지 않는 실란계 가스인 것을 특징으로 하는 산화 실리콘막의 성막 방법.The method according to claim 1,
Wherein the silicon raw material gas is an aminosilane-based gas or a silane-based gas not containing an amino group.
상기 아미노실란계 가스가,
BAS(부틸아미노실란)
BTBAS(비스터셔리부틸아미노실란)
DMAS(디메틸아미노실란)
BDMAS(비스디메틸아미노실란)
TDMAS(트리디메틸아미노실란)
DEAS(디에틸아미노실란)
BDEAS(비스디에틸아미노실란)
DPAS(디프로필아미노실란) 및,
DIPAS(디이소프로필아미노실란)
중 적어도 하나를 포함하는 가스로부터 선택되고,
상기 아미노기를 포함하지 않는 실란계 가스가,
SiH2
SiH4
SiH6
Si2H4
Si2H6
SimH2m +2(단, m은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물 및,
SinH2n(단, n은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물
중 적어도 하나를 포함하는 가스로부터 선택되는 것을 특징으로 하는 산화 실리콘막의 성막 방법.The method of claim 3,
Wherein the aminosilane-
BAS (butylaminosilane)
BTBAS (non-stearylbutylaminosilane)
DMAS (dimethylaminosilane)
BDMAS (bisdimethylaminosilane)
TDMAS (tridimethylaminosilane)
DEAS (diethylaminosilane)
BDEAS (bisdiethylaminosilane)
DPAS (dipropylaminosilane), and
DIPAS (diisopropylaminosilane)
≪ RTI ID = 0.0 > and / or < / RTI >
Wherein the silane-based gas containing no amino group,
SiH 2
SiH 4
SiH 6
Si 2 H 4
Si 2 H 6
Si m H 2m +2 (where m is a natural number of 3 or more)
Si n H 2n (where n is a natural number of 3 or more)
≪ / RTI > and a gas comprising at least one of the following.
상기 SimH2m +2(단, m은 3 이상의 자연수)의 식으로 나타나는 실리콘의 수소화물이,
트리실란(Si3H8)
테트라실란(Si4H10)
펜타실란(Si5H12)
헥사실란(Si6H14)
헵타실란(Si7H16)
중 적어도 하나로부터 선택되고,
상기 SinH2n(단, n은 3 이상의 자연수)의 식으로 나타나는 실리콘 수소화물이,
사이클로트리실란(Si3H6)
사이클로테트라실란(Si4H8)
사이클로펜타실란(Si5H10)
사이클로헥사실란(Si6H12)
사이클로헵타실란(Si7H14)
중 적어도 어느 하나로부터 선택되는 것을 특징으로 하는 산화 실리콘막의 성막 방법.5. The method of claim 4,
The hydride of silicon represented by the formula Si m H 2m +2 (where m is a natural number of 3 or more)
Trisilane (Si 3 H 8 )
Tetrasilane (Si 4 H 10 )
Pentasilane (Si 5 H 12 )
Hexasilane (Si 6 H 14 )
Heptasilane (Si 7 H 16 )
≪ / RTI >
The silicon hydride represented by the formula Si n H 2n (where n is a natural number of 3 or more)
Cyclotrisilane (Si 3 H 6 )
Cyclotetrasilane (Si 4 H 8 )
Cyclopentasilane (Si 5 H 10 )
Cyclohexasilane (Si 6 H 12 )
Cycloheptasilane (Si 7 H 14 )
Wherein the silicon oxide film is a silicon oxide film.
상기 성막 방법이 반도체 장치의 제조에 이용되는 것을 특징으로 하는 산화 실리콘막의 성막 방법.The method according to claim 1,
Wherein the film forming method is used for manufacturing a semiconductor device.
상기 제1 시드층 또는 상기 제2 시드층은 0.1nm 이상 0.3nm 이하의 두께를 갖는 것을 특징으로 하는 산화 실리콘막의 성막 방법.The method according to claim 1,
Wherein the first seed layer or the second seed layer has a thickness of 0.1 nm or more and 0.3 nm or less.
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US20120164327A1 (en) | 2012-06-28 |
TW201241226A (en) | 2012-10-16 |
TWI532871B (en) | 2016-05-11 |
KR20170057870A (en) | 2017-05-25 |
KR20150122108A (en) | 2015-10-30 |
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KR20120074207A (en) | 2012-07-05 |
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